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ID

24718

Beschrijving

Endocardial Stem Cells Approach Efficacy; ODM derived from: https://clinicaltrials.gov/show/NCT00841958

Link

https://clinicaltrials.gov/show/NCT00841958

Trefwoorden

Versies (1)
  1. 14-08-17 14-08-17 -
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14 augustus 2017

DOI

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Licentie

Creative Commons BY 4.0
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    Eligibility Myocardial Ischemia NCT00841958

    Engels

    Eligibility Myocardial Ischemia NCT00841958

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    men and women who are not of childbearing potential
    Beschrijving

    Childbearing Potential Absent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118
    UMLS CUI [1,2]
    C0332197
    age 21-75 years.
    Beschrijving

    Age

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    patients with cad, nyha and ccs angina iii-iv functional class
    Beschrijving

    Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Angina Pectoris Canadian Cardiovascular Society classification

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1956346
    UMLS CUI [2,1]
    C0002962
    UMLS CUI [2,2]
    C1275491
    UMLS CUI [3,1]
    C0002962
    UMLS CUI [3,2]
    C1277207
    lvef less than 35% measured by echocardiography or spect within three months of study entry
    Beschrijving

    Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction SPECT

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0428772
    UMLS CUI [1,2]
    C0013516
    UMLS CUI [2,1]
    C0428772
    UMLS CUI [2,2]
    C0040399
    unsuitable for initial or repeated conventional revascularization (cabg or pci)
    Beschrijving

    Inappropriate Revascularization Initial | Inappropriate Revascularization Repeated | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1548788
    UMLS CUI [1,2]
    C0581603
    UMLS CUI [1,3]
    C0205265
    UMLS CUI [2,1]
    C1548788
    UMLS CUI [2,2]
    C0581603
    UMLS CUI [2,3]
    C0205341
    UMLS CUI [3]
    C0010055
    UMLS CUI [4]
    C1532338
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    failure to provide informed consent.
    Beschrijving

    Informed Consent Lacking

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C0332268
    plan for pci or cabg.
    Beschrijving

    Percutaneous Coronary Intervention Planned | Coronary Artery Bypass Surgery Planned

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1532338
    UMLS CUI [1,2]
    C1301732
    UMLS CUI [2,1]
    C0010055
    UMLS CUI [2,2]
    C1301732
    non-cardiac illness with a life expectancy of less than 3 year.
    Beschrijving

    Illness | Exception Heart Diseases | Life Expectancy

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0221423
    UMLS CUI [2,1]
    C1705847
    UMLS CUI [2,2]
    C0018799
    UMLS CUI [3]
    C0023671
    conditions/circumstances likely to lead to poor treatment adherence (e.g., history of poor compliance, alcohol or drug dependency, psychiatric illness, no fixed abode).
    Beschrijving

    Condition Adherence to treatment plan Poor | Compliance behavior Poor | Substance Dependence | Mental disorders | No fixed abode

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0348080
    UMLS CUI [1,2]
    C0516958
    UMLS CUI [1,3]
    C0542537
    UMLS CUI [2,1]
    C1321605
    UMLS CUI [2,2]
    C0542537
    UMLS CUI [3]
    C0038580
    UMLS CUI [4]
    C0004936
    UMLS CUI [5]
    C0557219
    previous heart, kidney, liver, or lung transplantation.
    Beschrijving

    Heart Transplantation | Kidney Transplantation | Transplantation of liver | Lung Transplantation

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0018823
    UMLS CUI [2]
    C0022671
    UMLS CUI [3]
    C0023911
    UMLS CUI [4]
    C0024128
    current participation in another clinical trial in which a patient is taking an investigational drug or receiving an investigational medical device.
    Beschrijving

    Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    UMLS CUI [2]
    C0013230
    UMLS CUI [3]
    C2346570
    recent acute myocardial infarction (ami) within 90 days of study entry
    Beschrijving

    Myocardial Infarction

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0027051
    successful coronary revascularization (сabg or pci) within 12 months of study enrollment
    Beschrijving

    Coronary revascularisation Successful | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0877341
    UMLS CUI [1,2]
    C1272703
    UMLS CUI [2]
    C0010055
    UMLS CUI [3]
    C1532338
    history of moderate to severe aortic stenosis or prosthetic aortic valve
    Beschrijving

    Aortic Valve Stenosis Moderate | Aortic stenosis, severe | Aortic valve prosthesis

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0003507
    UMLS CUI [1,2]
    C0205081
    UMLS CUI [2]
    C3806272
    UMLS CUI [3]
    C0182431
    permanent atrial fibrillation
    Beschrijving

    Permanent atrial fibrillation

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2586056
    thrombosis in lv, based on echocardiography data
    Beschrijving

    Left ventricular thrombosis Echocardiography

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0587044
    UMLS CUI [1,2]
    C0013516
    Terug naar het begin van de pagina

    Similar models

    Eligibility Myocardial Ischemia NCT00841958

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Childbearing Potential Absent
    Item
    men and women who are not of childbearing potential
    boolean
    C3831118 (UMLS CUI [1,1])
    C0332197 (UMLS CUI [1,2])
    Age
    Item
    age 21-75 years.
    boolean
    C0001779 (UMLS CUI [1])
    Coronary Artery Disease | Angina Pectoris New York Heart Association Classification | Angina Pectoris Canadian Cardiovascular Society classification
    Item
    patients with cad, nyha and ccs angina iii-iv functional class
    boolean
    C1956346 (UMLS CUI [1])
    C0002962 (UMLS CUI [2,1])
    C1275491 (UMLS CUI [2,2])
    C0002962 (UMLS CUI [3,1])
    C1277207 (UMLS CUI [3,2])
    Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction SPECT
    Item
    lvef less than 35% measured by echocardiography or spect within three months of study entry
    boolean
    C0428772 (UMLS CUI [1,1])
    C0013516 (UMLS CUI [1,2])
    C0428772 (UMLS CUI [2,1])
    C0040399 (UMLS CUI [2,2])
    Inappropriate Revascularization Initial | Inappropriate Revascularization Repeated | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
    Item
    unsuitable for initial or repeated conventional revascularization (cabg or pci)
    boolean
    C1548788 (UMLS CUI [1,1])
    C0581603 (UMLS CUI [1,2])
    C0205265 (UMLS CUI [1,3])
    C1548788 (UMLS CUI [2,1])
    C0581603 (UMLS CUI [2,2])
    C0205341 (UMLS CUI [2,3])
    C0010055 (UMLS CUI [3])
    C1532338 (UMLS CUI [4])
    Item Group
    C0680251 (UMLS CUI)
    Informed Consent Lacking
    Item
    failure to provide informed consent.
    boolean
    C0021430 (UMLS CUI [1,1])
    C0332268 (UMLS CUI [1,2])
    Percutaneous Coronary Intervention Planned | Coronary Artery Bypass Surgery Planned
    Item
    plan for pci or cabg.
    boolean
    C1532338 (UMLS CUI [1,1])
    C1301732 (UMLS CUI [1,2])
    C0010055 (UMLS CUI [2,1])
    C1301732 (UMLS CUI [2,2])
    Illness | Exception Heart Diseases | Life Expectancy
    Item
    non-cardiac illness with a life expectancy of less than 3 year.
    boolean
    C0221423 (UMLS CUI [1])
    C1705847 (UMLS CUI [2,1])
    C0018799 (UMLS CUI [2,2])
    C0023671 (UMLS CUI [3])
    Condition Adherence to treatment plan Poor | Compliance behavior Poor | Substance Dependence | Mental disorders | No fixed abode
    Item
    conditions/circumstances likely to lead to poor treatment adherence (e.g., history of poor compliance, alcohol or drug dependency, psychiatric illness, no fixed abode).
    boolean
    C0348080 (UMLS CUI [1,1])
    C0516958 (UMLS CUI [1,2])
    C0542537 (UMLS CUI [1,3])
    C1321605 (UMLS CUI [2,1])
    C0542537 (UMLS CUI [2,2])
    C0038580 (UMLS CUI [3])
    C0004936 (UMLS CUI [4])
    C0557219 (UMLS CUI [5])
    Heart Transplantation | Kidney Transplantation | Transplantation of liver | Lung Transplantation
    Item
    previous heart, kidney, liver, or lung transplantation.
    boolean
    C0018823 (UMLS CUI [1])
    C0022671 (UMLS CUI [2])
    C0023911 (UMLS CUI [3])
    C0024128 (UMLS CUI [4])
    Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
    Item
    current participation in another clinical trial in which a patient is taking an investigational drug or receiving an investigational medical device.
    boolean
    C2348568 (UMLS CUI [1])
    C0013230 (UMLS CUI [2])
    C2346570 (UMLS CUI [3])
    Myocardial Infarction
    Item
    recent acute myocardial infarction (ami) within 90 days of study entry
    boolean
    C0027051 (UMLS CUI [1])
    Coronary revascularisation Successful | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
    Item
    successful coronary revascularization (сabg or pci) within 12 months of study enrollment
    boolean
    C0877341 (UMLS CUI [1,1])
    C1272703 (UMLS CUI [1,2])
    C0010055 (UMLS CUI [2])
    C1532338 (UMLS CUI [3])
    Aortic Valve Stenosis Moderate | Aortic stenosis, severe | Aortic valve prosthesis
    Item
    history of moderate to severe aortic stenosis or prosthetic aortic valve
    boolean
    C0003507 (UMLS CUI [1,1])
    C0205081 (UMLS CUI [1,2])
    C3806272 (UMLS CUI [2])
    C0182431 (UMLS CUI [3])
    Permanent atrial fibrillation
    Item
    permanent atrial fibrillation
    boolean
    C2586056 (UMLS CUI [1])
    Left ventricular thrombosis Echocardiography
    Item
    thrombosis in lv, based on echocardiography data
    boolean
    C0587044 (UMLS CUI [1,1])
    C0013516 (UMLS CUI [1,2])
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